Abstract
Most patients with suicide risk do not receive recommendations to reduce access to lethal means due to a variety of barriers (e.g., lack of provider time, training). Determine if highly efficient population-based EHR messaging to visit the Lock to Live (L2L) decision aid impacts patient-reported storage behaviors. Randomized trial. Integrated health care system serving Denver, CO. Served by primary care or mental health specialty clinic in the 75–99.5th risk percentile on a suicide attempt or death prediction model. Lock to Live (L2L) is a web-based decision aid that incorporates patients’ values into recommendations for safe storage of lethal means, including firearms and medications. Anonymous survey that determined readiness to change: pre-contemplative (do not believe in safe storage), contemplative (believe in safe storage but not doing it), preparation (planning storage changes) or action (safely storing). There were 21,131 patients randomized over a 6-month period with a 27% survey response rate. Many (44%) had access to a firearm, but most of these (81%) did not use any safe firearm storage behaviors. Intervention patients were more likely to be categorized as preparation or action compared to controls for firearm storage (OR = 1.30 (1.07–1.58)). When examining action alone, there were no group differences. There were no statistically significant differences for any medication storage behaviors. Selection bias in those who responded to survey. Efficiently sending an EHR invitation message to visit L2L encouraged patients with suicide risk to consider safer firearm storage practices, but a stronger intervention is needed to change storage behaviors. Future studies should evaluate whether combining EHR messaging with provider nudges (e.g., brief clinician counseling) changes storage behavior.
ClinicalTrials.gov: NCT05288517.
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Data Availability
De-identified trial data are available by request for scientific research only.
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Kaiser Permanente’s Office of Community Health as part of their Firearm Injury Prevention Program. The Kaiser Permanente Office of Community Health had no role in the design or conduct of the study; collection, management, analysis, or interpretation of the data; preparation of the manuscript; or the decision to submit the manuscript for publication. Per contract, the office reviewed the manuscript prior to submission for publication, but did not request (and cannot require) any changes.
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This study was reviewed and approved by the Kaiser Permanente Institutional Review Board. All patients who completed surveys provided informed consent. This study was performed in accordance with the ethical standards of the 1964 Declaration of Helsinki and its later amendments.
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Boggs, J.M., Quintana, L.M., Beck, A. et al. A Randomized Control Trial of a Digital Health Tool for Safer Firearm and Medication Storage for Patients with Suicide Risk. Prev Sci 25, 358–368 (2024). https://doi.org/10.1007/s11121-024-01641-6
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DOI: https://doi.org/10.1007/s11121-024-01641-6